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SLC26A2 - solute carrier family 26 member 2
- Synonym(s) : DTDST
- Previous symbols and names : 'solute carrier family 26 (sulfate transporter), member 2', DTD, Solute carrier family 26 (sulfate transporter), member 2, solute carrier family 26 (anion exchanger), member 2
- Type : gene with protein product
- Chromosomal location : 5q32
- OMIM: 606718
- HGNC: 10994
- UniProtKB: P50443
- Genatlas: SLC26A2
- GenCC: SLC26A2
- Ensembl: ENSG00000155850
- IUPHAR-DB: 1098
- Reactome: P50443
- LOVD: SLC26A2
Diseases list
- Disease-causing germline mutation(s) in Achondrogenesis type 1B
ORPHA:93298 
- Disease-causing germline mutation(s) in Atelosteogenesis type II
ORPHA:56304 - Disease-causing germline mutation(s) in Multiple epiphyseal dysplasia type 4
ORPHA:93307 - Disease-causing germline mutation(s) (loss of function) in Diastrophic dysplasia
ORPHA:628
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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